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It is considered a rare genetic condition and is associated with a wide range of clinical stigmata, such as short stature, ovarian dysgenesis, delayed puberty and infertility, congenital malformations, endocrine disorders, including a range of autoimmune conditions and type 2 diabetes, and neurocognitive deficits. Morbidity and mortality are clearly increased compared with the general population and the average age at diagnosis is quite delayed. During recent years it has become clear that a multidisciplinary approach is necessary toward the patient with TS. A number of clinical advances has been implemented, and these are reviewed. Our understanding of the genomic architecture of TS is advancing rapidly, and these latest developments are reviewed and discussed. Several candidate genes, genomic pathways and mechanisms, including an altered transcriptome and epigenome, are also presented.<\/jats:p>","DOI":"10.1210\/endrev\/bnac016","type":"journal-article","created":{"date-parts":[[2022,6,13]],"date-time":"2022-06-13T13:42:48Z","timestamp":1655127768000},"page":"33-69","source":"Crossref","is-referenced-by-count":139,"title":["The Changing Face of Turner Syndrome"],"prefix":"10.1210","volume":"44","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5924-1720","authenticated-orcid":false,"given":"Claus H","family":"Gravholt","sequence":"first","affiliation":[{"name":"Department of Endocrinology and Internal Medicine, Aarhus University Hospital , Aarhus 8200 N , Denmark"},{"name":"Department of Molecular Medicine, Aarhus University Hospital , Aarhus 8200 N , 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